FDA.reportPublic FDA data

De La Cruz Tincture of Iodine

Manufacturer
DLC Laboratories, Inc. | Pharma Nobis, LLC
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:04:35

Label at a glance#

ProductDe La Cruz Tincture of Iodine
Active ingredientIODINE, SODIUM IODIDE, ALCOHOL
Label structure13 sections

Dosage and administration

clean the affected area apply a small amount on the area 1 to 3 times daily may be covered with sterile bandage if bandaged let dry first

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Iodine 2%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Iodide 2.4%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 47%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Indications

INDICATIONS & USAGE SECTION

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings      

WARNINGS SECTION

For external use only.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns
  • Flammable: Keep away from sparks heat and flame

Stop use and consult doctor if

OTC - STOP USE SECTION

  • the condition persists or gets worse, or if using for longer than one week

When using this product

OTC - WHEN USING SECTION

  • do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids
  • do not apply over large areas of the body

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply a small amount on the area 1 to 3 times daily
  • may be covered with sterile bandage
  • if bandaged let dry first

Other information

OTHER SAFETY INFORMATION

  • will stain skin and clothing

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dlciod.jpgdlciod.jpglabellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24286-1528-7De La Cruz Tincture of Iodine30 mL in 1 BOTTLELIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24286-1528DE LA CRUZ TINCTURE OF IODINE (IODINE AND SODIUM IODIDE AND ALCOHOL) LIQUID [DLC LABORATORIES, INC.]5Current NDC, Legacy NDC, 1 package rows20231216_5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24286-152824286-1528-7

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
IODINE9679TC07X4ACTIB
SODIUM IODIDEF5WR8N145CACTIM
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
De La Cruz Tincture of IodineIODINE AND SODIUM IODIDE AND ALCOHOLDLC Laboratories, Inc.5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b2023-12-15WarningsExact identifier
ndc (package): 24286-1528-7
ndc (product): 24286-1528
ndc11 (package): 24286152807
spl id: 0c940d4f-cca2-7175-e063-6394a90af568
spl set id: 5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.